Medical Device Manufacturer · LI , Triesen

Bemer Int AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bemer Int AG General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Sep 23, 2023

B.Light Clear Evo and B.Light Restore Evo

General & Plastic Surgery · 268d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 15, 2026